Canonical Allele Identifier: CA2245701901
Gene: ACADVL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7222358G= , CM000679.2:g.7222358G= GRCh38
NC_000017.10:g.7125677G= , CM000679.1:g.7125677G= GRCh37
NC_000017.9:g.7066401G= NCBI36
NG_007975.1:g.7525G=
NG_008391.2:g.2693C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.878+56G= MANE Select ENSP00000349297.5:n.878+56G=
ENST00000322910.9:c.*833+56G= ENSP00000325395.5:n.*833+56G=
ENST00000350303.9:c.812+56G= ENSP00000344152.5:n.812+56G=
ENST00000356839.9:c.878+56G= ENSP00000349297.5:n.878+56G=
ENST00000543245.6:c.947+56G= ENSP00000438689.2:n.947+56G=
ENST00000577191.5:n.1106G=
ENST00000581378.5:c.596+56G=
ENST00000582379.1:n.262+56G=
NM_000018.3:c.878+56G= NP_000009.1:n.878+56G=
NM_001033859.2:c.812+56G= NP_001029031.1:n.812+56G=
NM_001270447.1:c.947+56G= NP_001257376.1:n.947+56G=
NM_001270448.1:c.650+56G= NP_001257377.1:n.650+56G=
XM_006721516.2:c.878+56G= XP_006721579.2:n.878+56G=
XM_011523829.1:c.878+56G= XP_011522131.1:n.878+56G=
XM_011523830.1:c.878+56G= XP_011522132.1:n.878+56G=
XR_934021.1:n.985+56G=
XR_934022.1:n.985+56G=
XR_934023.1:n.985+56G=
XM_006721516.3:c.878+56G= XP_006721579.2:n.878+56G=
XM_011523829.2:c.878+56G= XP_011522131.1:n.878+56G=
XM_011523830.2:c.878+56G= XP_011522132.1:n.878+56G=
XM_024450741.1:c.878+56G= XP_024306509.1:n.878+56G=
XR_934021.2:n.937+56G=
XR_934022.2:n.937+56G=
XR_934023.2:n.937+56G=
NM_000018.4:c.878+56G= MANE Select NP_000009.1:n.878+56G=
NM_001033859.3:c.812+56G= NP_001029031.1:n.812+56G=
NM_001270447.2:c.947+56G= NP_001257376.1:n.947+56G=
NM_001270448.2:c.650+56G= NP_001257377.1:n.650+56G=
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